Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

94 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Molecular investigation of distal renal tubular acidosis in Tunisia, evidence for founder mutations.
Nagara M, Voskarides K, Nouira S, Ben Halim N, Kefi R, Aloulou H, Romdhane L, Ben Abdallah R, Ben Rhouma F, Aissa K, Boughamoura L, Kammoun T, Azzouz H, Abroug S, Ben Turkia H, Ayadi A, Mrad R, Chabchoub I, Hachicha M, Chemli J, Deltas C, Abdelhak S. Nagara M, et al. Among authors: azzouz h. Genet Test Mol Biomarkers. 2014 Nov;18(11):741-8. doi: 10.1089/gtmb.2014.0175. Epub 2014 Oct 6. Genet Test Mol Biomarkers. 2014. PMID: 25285676 Free PMC article. Clinical Trial.
Molecular and biochemical characterization of a novel intronic single point mutation in a Tunisian family with glycogen storage disease type III.
Ben Rhouma F, Azzouz H, Petit FM, Khelifa MB, Chehida AB, Nasrallah F, Parisot F, Lasram K, Kefi R, Bouyacoub Y, Romdhane L, Baussan C, Kaabachi N, Ben Dridi MF, Tebib N, Abdelhak S. Ben Rhouma F, et al. Among authors: azzouz h. Mol Biol Rep. 2013 Jul;40(7):4197-202. doi: 10.1007/s11033-013-2500-z. Epub 2013 May 8. Mol Biol Rep. 2013. PMID: 23649758
History of settlement of villages from Central Tunisia by studying families sharing a common founder Glycogenosis type III mutation.
Rhouma FB, Messai H, Hsouna S, Halim NB, Cherif W, Fadhel SB, Tiar A, Nagara M, Azzouz H, Sfar MT, Dridi MF, Tebib N, Ayadi A, Abdelhak S, Kefi R. Rhouma FB, et al. Among authors: azzouz h. Mitochondrial DNA A DNA Mapp Seq Anal. 2016 Sep;27(5):3194-8. doi: 10.3109/19401736.2015.1007331. Epub 2015 Dec 24. Mitochondrial DNA A DNA Mapp Seq Anal. 2016. PMID: 26704523
Mutation spectrum of glycogen storage disease type Ia in Tunisia: implication for molecular diagnosis.
Barkaoui E, Cherif W, Tebib N, Charfeddine C, Ben Rhouma F, Azzouz H, Ben Chehida A, Monastiri K, Chemli J, Amri F, Ben Turkia H, Abdelmoula MS, Kaabachi N, Abdelhak S, Ben Dridi MF. Barkaoui E, et al. Among authors: azzouz h. J Inherit Metab Dis. 2007 Nov;30(6):989. doi: 10.1007/s10545-007-0737-1. Epub 2007 Nov 19. J Inherit Metab Dis. 2007. PMID: 18008183
Screening of three Mediterranean phenylketonuria mutations in Tunisian families.
Khemir S, Siala H, Taieb SH, Cherif W, Azzouz H, Kéfi R, Abdelhak S, Khouja N, Tebib N, Massaoud T, Ben Dridi MF, Kaabachi N. Khemir S, et al. Among authors: azzouz h. J Genet. 2012;91(1):91-4. doi: 10.1007/s12041-012-0140-z. J Genet. 2012. PMID: 22546830 Free article. No abstract available.
Clinical and Genetic Characterization of 26 Tunisian Patients with Allgrove Syndrome.
Kallabi F, Belghuith N, Aloulou H, Kammoun T, Ghorbel S, Hajji M, Gallas S, Chemli J, Chabchoub I, Azzouz H, Ben Chehida A, Sfaihi L, Makni S, Amouri A, Keskes L, Tebib N, Ben Becher S, Hachicha M, Kamoun H. Kallabi F, et al. Among authors: azzouz h. Arch Med Res. 2016 Feb;47(2):105-10. doi: 10.1016/j.arcmed.2016.04.004. Epub 2016 Apr 28. Arch Med Res. 2016. PMID: 27133709
Homogénéité mutationnelle de la glycogénose de type Ia en Tunisie.
Cherif W, Rhouma FB, Chehida AB, Azzouz H, Monastiri K, Amri F, Chemli J, Kaabachi N, Abdelhak S, Tebib N, Dridi MF. Cherif W, et al. Among authors: azzouz h. Pathol Biol (Paris). 2011 Aug;59(4):e93-6. doi: 10.1016/j.patbio.2009.05.004. Epub 2009 Nov 5. Pathol Biol (Paris). 2011. PMID: 19896294
94 results